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Chemistry

D-Index
50
Citations
7534
World Ranking
14541
National Ranking
96

Overview

Herfried Griengl is affiliated with Graz University of Technology in Austria, where their research focuses on fields related to biochemistry, genetics, molecular biology, and engineering.

The primary areas of study for Griengl include:

  • Biochemistry, Genetics and Molecular Biology
  • Engineering

More specifically, their subfields of research encompass:

  • Molecular Biology
  • Biomedical Engineering

Griengl's work covers several main research topics, such as:

  • Enzyme Catalysis and Immobilization
  • Microbial Metabolic Engineering and Bioproduction
  • Biofuel production and bioconversion

Their recent publication activity includes a paper titled Biocatalytic Friedel-Crafts alkylation, published in 2022 in the TUGraz OPEN Library (Graz University of Technology).

Their frequent collaborators include:

  • Harald Stecher
  • Martin Tengg
  • Peter Remler
  • Helmut Schwab
  • Mandana Gruber

Most of Griengl's publications have appeared in the TUGraz OPEN Library at Graz University of Technology.

Best Publications

  • De‐racemization of Enantiomers versus De‐epimerization of Diastereomers—Classification of Dynamic Kinetic Asymmetric Transformations (DYKAT)

    Johannes Steinreiber;Kurt Faber;Herfried Griengl

  • HIGH-LEVEL INTRACELLULAR EXPRESSION OF HYDROXYNITRILE LYASE FROM THE TROPICAL RUBBER TREE HEVEA BRASILIENSIS IN MICROBIAL HOSTS

    Meinhard Hasslacher;Michael Schall;Marianne Hayn;Rudolfo Bona

  • Oxidative biotransformations using oxygenases.

    Zhi Li;Jan B van Beilen;Wouter A Duetz;Andreas Schmid

  • A Biocatalytic Henry Reaction—The Hydroxynitrile Lyase from Hevea brasiliensis Also Catalyzes Nitroaldol Reactions

    Thomas Purkarthofer;Karl Gruber;Mandana Gruber-Khadjawi;Kerstin Waich

  • Molecular Cloning of the Full-length cDNA of (S)-Hydroxynitrile Lyase from Hevea brasiliensis FUNCTIONAL EXPRESSION IN ESCHERICHIA COLI AND SACCHAROMYCES CEREVISIAE AND IDENTIFICATION OF AN ACTIVE SITE RESIDUE

    Meinhard Hasslacher;Michael Schall;Marianne Hayn;Herfried Griengl

  • Biocatalytic Friedel-Crafts alkylation using non-natural cofactors.

    Harald Stecher;Martin Tengg;Bernhard J. Ueberbacher;Peter Remler

  • Potential and capabilities of hydroxynitrile lyases as biocatalysts in the chemical industry

    Thomas Purkarthofer;Wolfgang Skranc;Christian Schuster;Herfried Griengl

  • Hydroxynitrile lyase-catalyzed enzymatic nitroaldol (henry) reaction

    Mandana Gruber-Khadjawi;Thomas Purkarthofer;Wolfgang Skranc;Herfried Griengl

  • The synthesis of chiral cyanohydrins by oxynitrilases

    Herfried Griengl;Helmut Schwab;Martin Fechter

  • Hydroxynitrile lyases : Functions and properties

    Andrea Hickel;Meinhard Hasslacher;Herfried Griengl

  • Mechanism of cyanogenesis: the crystal structure of hydroxynitrile lyase from Hevea brasiliensis

    UG Wagner;M Hasslacher;H Griengl;H Schwab

  • Enzymatic cleavage and formation of cyanohydrins: a reaction of biological and synthetic relevance

    Herfried Griengl;Andrea Hickel;Dean V. Johnson;Michael Schmidt

  • ENZYME CATALYSED FORMATION OF (S)-CYANOHYDRINS DERIVED FROM ALDEHYDES AND KETONES IN A BIPHASIC SOLVENT SYSTEM

    Herfried Griengl;Norbert Klempier;Peter Pöchlauer;Michael Schmidt

  • Threonine aldolases—an emerging tool for organic synthesis

    Johannes Steinreiber;Kateryna Fesko;Christoph Reisinger;Martin Schürmann

  • Preparation of optically active cyanohydrins using the (S)-hydroxynitrile lyase from Hevea brasiliensis

    Michael Schmidt;Stephanie Hervé;Norbert Klempier;Herfried Griengl

  • Oxynitrilases: From Cyanogenesis to Asymmetric Synthesis

    Michael Schmidt;Herfried Griengl

  • Aliphatic (S)-cyanohydrins by enzyme catalyzed synthesis

    Norbert Klempier;Herfried Griengl;Marianne Hayn

  • Enzymatic resolution of norbornane-type esters

    Th. Oberhauser;M. Bodenteich;K. Faber;G. Penn

  • 5-(Haloalkyl)-2'-deoxyuridines: a novel type of potent antiviral nucleoside analogue.

    Griengl H;Bodenteich M;Hayden W;Wanek E

  • Enzymatic acylation using acid anhydrides: Crucial removal of acid

    B. Berger;C.G. Rabiller;K. Königsberger;K. Faber

Frequent Co-Authors

Kurt Faber
Kurt Faber University of Graz
Karl Gruber
Karl Gruber University of Graz
Sepp D. Kohlwein
Sepp D. Kohlwein University of Graz
Erik De Clercq
Erik De Clercq Rega Institute for Medical Research
Sergio Riva
Sergio Riva National Research Council (CNR)
Andreas Liese
Andreas Liese Hamburg University of Technology
Frances H. Arnold
Frances H. Arnold California Institute of Technology
Jan Balzarini
Jan Balzarini KU Leuven
Vladimir Kren
Vladimir Kren Czech Academy of Sciences
Roland Furstoss
Roland Furstoss Centre national de la recherche scientifique, CNRS

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